2-(5-(1,1-dimethylethoxy)-5-oxopent-1-ynyl)-cyclopentene-1-carboxylic acid | 1192253-50-1

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 2-(5-(1,1-dimethylethoxy)-5-oxopent-1-ynyl)-cyclopentene-1-carboxylic acid
• CAS: 1192253-50-1
• 化学式: C₁₅H₂₀O₄
• 分子量: 264.321
• InChiKey: WSDQZLVOPKYHSR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.68
• 重原子数：
  19.0
• 可旋转键数：
  3.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  63.6
• 氢给体数：
  1.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  2-(5-(1,1-dimethylethoxy)-5-oxopent-1-ynyl)-cyclopentene-1-carboxylic acid 、 H-Phe-pNA*HCl 在 benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 24.0h， 以88%的产率得到N-(2-(5-(1,1-dimethylethoxy)-5-oxopent-1-ynyl)-cyclopentene-1-carbonyl)-L-phenylalanine N-(4-nitrophenyl)amide
  参考文献：
  名称：

  Synthesis of 2-(4-carboxybutenyl)- and 2-(4-carboxybutynyl)-cyclopentene-1-carboxamides

  摘要：

  Syntheses of 2-(4-carboxybut-1-enyl/4-carboxypent-1-ynyl)cyclopentene-1-carboxamides, compounds designed to mimic the phosphoSer-Pro dipeptide motif (the recognition sequence for the prolyl cis-trans isomerase Pin1), have been developed. Stille, Sonogashira and Suzuki couplings were envisaged to join the pentynoic and pentenoic acid side chains to the 2-position of cyclopentene-1-carboxylate esters. The ring- and side-chain carboxylic acids required orthogonal protection for later attachment of a Ph-NH(4-nitrophenyl) unit to the cyclopentene-1-carbonyl. The cyclopentenecarboxylates were unmasked and standard PyBOP peptide coupling afforded the target compounds. Comparisons of two routes using Bur and Me esters are reported. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2009.07.085
• 作为产物：
  描述：

  methyl 2-(5-(1,1-dimethylethoxy)-5-oxopent-1-ynyl)cyclopent-1-enecarboxylate 在 lithium hydroxide monohydrate 、 水 、 硫酸 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 16.0h， 以5%的产率得到2-(5-(1,1-dimethylethoxy)-5-oxopent-1-ynyl)-cyclopentene-1-carboxylic acid
  参考文献：
  名称：

  Synthesis of 2-(4-carboxybutenyl)- and 2-(4-carboxybutynyl)-cyclopentene-1-carboxamides

  摘要：

  Syntheses of 2-(4-carboxybut-1-enyl/4-carboxypent-1-ynyl)cyclopentene-1-carboxamides, compounds designed to mimic the phosphoSer-Pro dipeptide motif (the recognition sequence for the prolyl cis-trans isomerase Pin1), have been developed. Stille, Sonogashira and Suzuki couplings were envisaged to join the pentynoic and pentenoic acid side chains to the 2-position of cyclopentene-1-carboxylate esters. The ring- and side-chain carboxylic acids required orthogonal protection for later attachment of a Ph-NH(4-nitrophenyl) unit to the cyclopentene-1-carbonyl. The cyclopentenecarboxylates were unmasked and standard PyBOP peptide coupling afforded the target compounds. Comparisons of two routes using Bur and Me esters are reported. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2009.07.085